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Living on the edge with too many mouths to feed: Why dopamine neurons die
Although genes, protein aggregates, environmental toxins, and other factors associated with Parkinson’s disease (PD) are widely distributed in the nervous system and affect many classes of neurons, a consistent feature of PD is the exceptional and selective vulnerability of dopamine (DA) neurons of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504389/ https://www.ncbi.nlm.nih.gov/pubmed/23008164 http://dx.doi.org/10.1002/mds.25135 |
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author | Bolam, J Paul Pissadaki, Eleftheria K |
author_facet | Bolam, J Paul Pissadaki, Eleftheria K |
author_sort | Bolam, J Paul |
collection | PubMed |
description | Although genes, protein aggregates, environmental toxins, and other factors associated with Parkinson’s disease (PD) are widely distributed in the nervous system and affect many classes of neurons, a consistent feature of PD is the exceptional and selective vulnerability of dopamine (DA) neurons of the SNc. What is it about these neurons, among all other neurons in the brain, that makes them so susceptible in PD? We hypothesize that a major contributory factor is the unique cellular architecture of SNc DA neuron axons. Their large, complex axonal arbour puts them under such a tight energy budget that it makes them particularly susceptible to factors that contribute to cell death, including unique molecular characteristics associated with SNc DA neurons and nonspecific, nervous-system–wide factors. © 2012 Movement Disorder Society |
format | Online Article Text |
id | pubmed-3504389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-35043892012-11-30 Living on the edge with too many mouths to feed: Why dopamine neurons die Bolam, J Paul Pissadaki, Eleftheria K Mov Disord Viewpoints Although genes, protein aggregates, environmental toxins, and other factors associated with Parkinson’s disease (PD) are widely distributed in the nervous system and affect many classes of neurons, a consistent feature of PD is the exceptional and selective vulnerability of dopamine (DA) neurons of the SNc. What is it about these neurons, among all other neurons in the brain, that makes them so susceptible in PD? We hypothesize that a major contributory factor is the unique cellular architecture of SNc DA neuron axons. Their large, complex axonal arbour puts them under such a tight energy budget that it makes them particularly susceptible to factors that contribute to cell death, including unique molecular characteristics associated with SNc DA neurons and nonspecific, nervous-system–wide factors. © 2012 Movement Disorder Society Wiley Subscription Services, Inc., A Wiley Company 2012-09 2012-10 /pmc/articles/PMC3504389/ /pubmed/23008164 http://dx.doi.org/10.1002/mds.25135 Text en Copyright © 2012 Movement Disorder Society http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Viewpoints Bolam, J Paul Pissadaki, Eleftheria K Living on the edge with too many mouths to feed: Why dopamine neurons die |
title | Living on the edge with too many mouths to feed: Why dopamine neurons die |
title_full | Living on the edge with too many mouths to feed: Why dopamine neurons die |
title_fullStr | Living on the edge with too many mouths to feed: Why dopamine neurons die |
title_full_unstemmed | Living on the edge with too many mouths to feed: Why dopamine neurons die |
title_short | Living on the edge with too many mouths to feed: Why dopamine neurons die |
title_sort | living on the edge with too many mouths to feed: why dopamine neurons die |
topic | Viewpoints |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504389/ https://www.ncbi.nlm.nih.gov/pubmed/23008164 http://dx.doi.org/10.1002/mds.25135 |
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